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Título: Vaccination with formulation of nanoparticles loaded with Leishmania amazonensis antigens confers protection against experimental visceral Leishmaniasis in hamster
Autores: Cabrera González, Marco Antonio 
Maia Gonçalves, Ana Alice 
Ottino, Jennifer 
Costa Leite, Jaqueline 
Aparecida Resende, Lucilene 
Melo Júnior, Otoni Alves 
Silveira, Patrícia 
Santos Cardoso, Mariana 
Toshio Fujiwara, Ricardo 
Lacerda Bueno, Lilian 
Lima Santos, Renato 
Furtado de Carvalho, Tatiane 
Martins Garcia, Giani 
de Oliveira Paes, Paulo Ricardo 
Sobreira Galdino, Alexsandro 
Chávez Fumagalli, Miguel Angel 
Martins Melo, Marília 
Silveira Lemos, Denise 
Martins Filho, Olindo Assis 
Ornelas Dutra, Walderez 
Furtado Mosqueira, Vanessa Carla 
Cordeiro Giunchetti, Rodolfo 
Palabras clave: Visceral leishmaniasis, Nanotechnology, Vaccine
Fecha de emisión: 2-ene-2023
Editor: MDPI
Fuente: González, M.; Gonçalves, A.; Ottino, J.; Leite, J.; Resende, L.; Melo, O.; Silveira, P.; Cardoso, M.; Fujiwara, R.; Bueno, L.; Santos, R.; Carvalho, T.; Garcia, G.; Paes.; Galdino, A.; Chávez, M.; Melo, M.; Silveira, D.; Martins, O.; … Giunchetti, R. (2023). Vaccination with formulation of nanoparticles loaded with Leishmania amazonensis antigens confers protection against experimental visceral Leishmaniasis in hamster. Vaccines, 11(1), 111. doi: 10.3390/vaccines11010111
Revista: Vaccines 
Resumen: 
Visceral leishmaniasis (VL) is a fatal disease caused by the protozoa Leishmania infantum for which dogs are the main reservoirs. A vaccine against canine visceral leishmaniasis (CVL) could be an important tool in the control of human and CVL by reducing the infection pressure of L. infantum. Despite the CVL vaccine available on the market, the Brazilian Ministry of Health did not implement the use of it in their control programs. In this sense, there is an urgent need to develop more efficient vaccines. In this study, the association between two polymeric nanoformulations, (poly (D, L-lactic) acid (PLA) polymer) loading Leishmania amazonensis antigens, was evaluated as a potential immunobiological agent against VL using golden hamsters as an experimental model. The results indicated that no significant adverse reactions were observed in animals vaccinated with LAPSmP. LAPSmP presented similar levels of total anti-Leishmania IgG as compared to LAPSmG. The LAPSmP and LAPSmG groups showed an intense reduction in liver and spleen parasitic load by qPCR. The LAPSmP and LAPSmG vaccines showed exceptional results, indicating that they may be promising candidates as a VL vaccine.
URI: https://hdl.handle.net/20.500.12955/2090
DOI:  10.3390/vaccines11010111
Derechos: info:eu-repo/semantics/openAccess
Aparece en Colecciones:Artículos científicos

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